Translations in context of “Hiperlaxitud articular” in Spanish-English from Reverso Context: Leve curvatura espinal Hiperlaxitud articular deficiencia de los . También presentan hiperlaxitud articular, a veces con subluxaciones recurrentes , piel extensible y friable, con moretones fáciles y alteración ocular, con. El síndrome de hiperlaxitud articular (SHA) se caracteriza por la presencia de hiperlaxitud articular y síntomas en relación con el aparato locomotor. La etiología.
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síndrome de ehlers-danlos y síndrome de hiperlaxitud articular – | EDS | Pinterest
Se continuar a navegar, consideramos que aceita o seu uso. The most frequent symptom is the musculo-skeletal pain. Enfoques top-down y bottom-up para el tratamiento de la Surgical procedures should be considered with caution.
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Hiperlaxitud Articular | O_O | Guillermo Salinas | Flickr
CiteScore measures average citations received per document published. Genetic counseling Transmission is autosomal dominant. Complications often include chronic pain affecting physical activity, fatigue, sleep disorders, early osteoarthritis artidular osteoporosis, and cardiovascular symptoms chest pain, palpitations, postural instability.
It is not known whether penetrance is complete but there is highly variable expressivity.
Hyperlaxity is more pronounced in younger patients and in females. Its etiology is not absolutely well-known.
The underlying pathogenic mechanism is unknown.
Subscriber If you already have your login data, please click here. Supportive and symptomatic individualized hiperelasgicidad include physical therapy, rehabilitation, assistive devices, pain medications, and suitable therapy for extra-articular manifestations.
Artiicular primary manifestation is hyperlaxity involving any joints: Prognosis There is no increased risk of early mortality but high morbidity due to joint hyperlaxity, chronic and acute pain as well as extra-musculoskeletal manifestations which all greatly diminish quality of life. Other diseases that also involve joint laxity are generally easy to distinguished from EDS by their characteristic features.
To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. You can change the settings or obtain more information by clicking here. The most frequent symptom is the musculoskeletal pain. Major diagnostic criteria include joint hyperlaxity, soft skin or skin hyperextensibility, and an absence of other significant skin or soft tissue fragility.
It does not have a specific treatment. Wide clinical variability is found. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined in the Villefranche classification. Transmission is autosomal dominant. Diagnostic methods Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined in the Villefranche classification. The diagnosis of this syndrome is clinical.
Onset can be at any age but it is difficult to assess in young children due to higher joint laxity at this age. However, the Villefranche classification does not take into account the extra-musculoskeletal manifestations.
SRJ is a prestige metric based on the idea that not all citations are the same.
Previous article Next article. Health care resources for this disease Expert centres Diagnostic tests 35 Patient organisations 42 Orphan drug s 0. These figures may however be underestimated due to clinical variability. Other search option s Alphabetical list. Print Send to a friend Export reference Mendeley Statistics.
Etiology The underlying pathogenic mechanism is unknown. Supportive diagnostic criteria include a positive family history, recurrent joint instability, and easy bruising.
Translation of “Hiperlaxitud articular” in English
Ehlers-Danlos syndrome, hypermobility type HT-EDS is the most frequent form of EDS see this terma group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations. Perucho Pont a. There is no increased risk of early mortality but high morbidity due to joint hyperlaxity, chronic and acute pain as well as extra-musculoskeletal manifestations which all greatly diminish quality of life.
Only comments written in English can be processed. Continuing navigation will be considered as acceptance of this use. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. In most cases, one or both parents of an affected individual have some degree of joint laxity, easy bruising, or soft skin, and some of these symptoms occasionally seem to segregate within the patient’s family.